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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2146생성일: 2026년 10월 26일

Triethylamine → 2-(3,4-Dimethoxybenzenesulphonyl)-4-(2-pyrid-2-ylethynyl)isoindoline

https://huagongshe.com/reaction/2146

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물EthynylpyridineHCID 137268—
반응물2-(3,4-Dimethoxybenzenesulphonyl)-4-bromoisoindolineHCID 19689661—
촉매PalladiumHCID 23938—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(3,4-Dimethoxybenzenesulphonyl)-4-(2-pyrid-2-ylethynyl)isoindolineHCID 1968964012.5%

반응 조건

온도90 °C

반응 단계

2-(3,4-Dimethoxybenzenesulphonyl)-4-bromoisoindoline (0.19 g), triethylamine (0.10 ml), 2-ethynylpyridine(0.06 g) and bis (triphenylphosphine)palladium(II)chloride (10%) in anhydrous N,N-dimethylformamide(2 ml) were stirred together under an inert atmosphere and heated to 90° C. After 20 hours further 2-ethynylpyridine(0.12 g) and palladium catalyst (20%) were added and heating continued for 3 days. The reaction mixture at room temperature was diluted with ethyl acetate, filtered through a pad of silica and the filtrate evaporated in vacuo to yield a yellow residue. Purification by column chromatography, eluting with a 20-100% ethyl acetate in hexane gradient afforded the title compound (25 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728712
출처 데이터셋uspto-grants-1998_03
ORD IDord-1fbe8bec2d7a4b37b8e811f839c2b36c
출처 메모uspto-grants-1998_03